Design and rationale for the Cardiovascular and Metabolic Effects of Lorcaserin in Overweight and Obese Patients-Thrombolysis in Myocardial Infarction 61 (CAMELLIA-TIMI 61) trial

被引:11
作者
Bohula, Erin A. [1 ]
Scirica, Benjamin M. [1 ]
Fanola, Christina [1 ]
Inzucchi, Silvio E. [2 ]
Keech, Anthony [3 ]
McGuire, Darren K. [4 ]
Smith, Steven R. [5 ]
Abrahamsen, Tim [1 ]
Francis, Bruce H. [6 ]
Miao, Wenfeng [6 ]
Perdomo, Carlos A. [6 ]
Satlin, Andrew [6 ]
Wiviott, Stephen D. [1 ]
Sabatine, Marc S. [1 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Dept Med, TIMI Study Grp,Cardiovasc Div, Boston, MA USA
[2] Yale Univ, Sch Med, New Haven, CT USA
[3] Univ Sydney, Natl Hlth & Med Res Council, Clin Trials Ctr, Sydney Med Sch, Sydney, NSW, Australia
[4] Univ Texas Southwestern Med Ctr Dallas, Dept Internal Med, Div Cardiol, Dallas, TX USA
[5] Florida Hosp, Translat Res Inst Metab & Diabet, Orlando, FL USA
[6] Eisai Inc, Woodcliff Lake, NJ USA
关键词
LIFE-STYLE INTERVENTION; BARIATRIC SURGERY; WEIGHT-LOSS; DIABETES-MELLITUS; RISK-FACTORS; PREVENTION; EVENTS; MULTICENTER; MORTALITY; OUTCOMES;
D O I
10.1016/j.ahj.2018.03.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Lorcaserin, a selective serotonin 2C receptor agonist, is an effective pharmacologic weight-loss therapy that improves several cardiovascular risk factors. The long-term clinical cardiovascular and metabolic safety and efficacy in patients with elevated cardiovascular risk are unknown. Research design and methods: CAMELLIA-TIMI 61 (NCT02019264) is a randomized, double-blind, placebo-controlled, multinational clinical trial designed to evaluate the safety and efficacy of lorcaserin with regard to major adverse cardiovascular events and progression to diabetes in overweight or obese patients at high cardiovascular risk. Overweight or obese patients either with established cardiovascular disease or with diabetes and at least 1 other cardiovascular risk factor were randomized in a 1:1 ratio to lorcaserin 10 mg twice daily or matching placebo. The primary safety objective is to assess for noninferiority of lorcaserin for the composite end point of cardiovascular death, myocardial infarction, or stroke (major adverse cardiovascular event [MACE]) (with noninferiority defined as the upper bound of a 1-sided 97.5% CI excluding a hazard ratio of 1.4) compared with placebo assessed at an interim analysis with 460 adjudicated events. The efficacy objectives, assessed at study completion, will evaluate the superiority of lorcaserin for the primary composite end point of cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina, heart failure, or any coronary revascularization (MACE+) and the key secondary end point of conversion to diabetes. Recruitment began in January 2014 and was completed in November 2015 resulting in a total population of 12,000 patients. The trial is planned to continue until at least 1,401 adjudicated MACE+ events are accrued and the median treatment duration exceeds 2.5 years. Conclusion: CAMELLIA-TIMI 61 is investigating the safety and efficacy of lorcaserin for MACEs and conversion to diabetes in overweight or obese patients with established cardiovascular disease or multiple cardiovascular risk factors. (C) 2018 Published by Elsevier Inc.
引用
收藏
页码:39 / 48
页数:10
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